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The European Commission proposed on 23 January more time for companies to apply the In Vitro Diagnostic Medical Devices Regulation (IVDR), under certain conditions, as well as measures to enhance transparency in the medical device sector including speeding up the launch of some elements of the European Database on Medical Devices - EUDAMED.
The European Commission proposed Tuesday to improve the availability of in vitro diagnostics and extend the time for companies to apply the In Vitro Diagnostics regulation.
A child plays outside the gates of a hotel used as temporary accommodation for families waiting for their asylum claims to be processed, in west London, February 16, 2021 © 2021 Justin Tallis/AFP via Getty Images Map UK CRD Map Summary The United Kingdom has historically provided housing support to people seeking asylum who arrive in the country and are not immediately able to provide for their own basic needs. In recent years this system has increasingly been plagued by serious deficiencies, in
To help laboratories prepare for the upcoming In Vitro Diagnostic Medical Devices Regulation (IVDR) and to clear up any confusion, Beckman Coulter Life Sciences has achieved an industry-first by offering more than 270 reagents for flow cytometry that are IVDR compliant and available immediately. Click to read more...
Beckman Coulter Life Sciences, a global leader in laboratory automation and innovation, is leading the way to help laboratories prepare for critical upgrades to comply with the new In Vitro Diagnostic Medical Devices Regulation (IVDR), and to clear up confusion for laboratories that will soon be governed by IVDR.